Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs4790953 0.851 0.160 17 65230912 downstream gene variant A/C snv 0.17 4
rs10494334 1.000 0.080 1 163535374 intergenic variant G/A snv 0.10 1
rs1867898 1.000 0.080 2 133762000 intergenic variant G/A snv 0.22 1
rs1986513 1.000 0.080 4 125146073 intergenic variant A/T snv 8.9E-02 1
rs4791746 1.000 0.080 17 8723039 intergenic variant T/A;C snv 1
rs9384169 1.000 0.080 6 153992036 intergenic variant T/C snv 0.36 1
rs9478495 1.000 0.080 6 154002774 intergenic variant G/A snv 0.19 1
rs965972 1.000 0.080 1 193494720 intron variant G/A snv 0.86 1
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs768020372
ALDH2
1.000 0.080 12 111792761 missense variant C/G;T snv 6.3E-06 1
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs2133896
ANKS1B
0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs2270162
AUTS2 ; CT66
1.000 0.080 7 69596980 intron variant C/G;T snv 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs13306221
BDNF
0.851 0.120 11 27701142 intron variant C/T snv 5.9E-02 4
rs16917204
BDNF-AS
0.827 0.160 11 27646808 intron variant G/C snv 0.17 5
rs11030096
BDNF-AS
0.925 0.160 11 27643996 intron variant T/A;C snv 3
rs7481311
BDNF-AS
0.925 0.160 11 27561582 intron variant T/C snv 0.75 2
rs988712
BDNF-AS
0.925 0.160 11 27541835 intron variant G/A;T snv 2
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs11030104
BDNF ; BDNF-AS
0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs16917234
BDNF ; BDNF-AS
0.925 0.080 11 27676827 intron variant T/A;C snv 2